Evidence map›Paper›PMID 17245434›Full record

ArticleThe EMBO journal2007

PSGL-1 and mTOR regulate translation of ROCK-1 and physiological functions of macrophages.

Richard Fox, Thomas Q Nhan, G Lynn Law, David R Morris, W Conrad Liles, Stephen M Schwartz

Erratum issuedOpen access · bronzeAbstract read
In one paragraph

Article in The EMBO journal, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
2.0field-weighted citation impact, top 14% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

38 citing papers in PubMed, 64 citations in OpenAlex.

  1. Trial
  2. mTOR Signaling in Macrophages: All Depends on the Context.International journal of molecular sciences · 2025
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4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

6 authors at 2 institutions in 2 countries.

Richard FoxDepartment of Pathology, University of Washington, Seattle, WA 98109, USA. richardfox.fox@gmail.com
Thomas Q Nhan
G Lynn Law
David R Morris
W Conrad Liles
Stephen M Schwartz
University of Washington · USUniversity Health Network · CA

Funding

Vasular cell origins and fates in granulation tissueP01HL003174 · NHLBI · UNIVERSITY OF WASHINGTON · PI SCHWARTZ, EMILY J. · 1985 to 2007
$13.8M
EXPERIMENTAL PATHOLOGY OF CARDIOVASCULAR DISEASET32HL007312 · NHLBI · UNIVERSITY OF WASHINGTON · PI MAJESKY, MARK W., SCHWARTZ, STEPHEN MARK · 1985 to 2019
$11.8M
Neovasculature, Plaque Rupture And Progression by MRIP01HL072262 · NHLBI · UNIVERSITY OF WASHINGTON · PI ROSSINI, ANTHONY J · 2002 to 2006
$11.5M
DEVELOPMENT OF TRANSLATION STATE ARRAY ANALYSISR33CA089807 · NCI · UNIVERSITY OF WASHINGTON · PI MORRIS, DAVID R · 2001 to 2003
$2.2M
NCI NIH HHS CA89807NCI NIH HHS R33 CA089807NHLBI NIH HHS HL07312NHLBI NIH HHS HL62945NHLBI NIH HHS HL72262NHLBI NIH HHS P01 HL003174NHLBI NIH HHS P01 HL03174NHLBI NIH HHS T32 HL007312
6 · The paper itself

Abstract

Rho-associated kinases (ROCKs) are critical molecules involved in the physiological functions of macrophages, such as chemotaxis and phagocytosis. We demonstrate that macrophage adherence promotes rapid changes in physiological functions that depend on translational upregulation of preformed ROCK-1 mRNA, but not ROCK-2 mRNA. Before adherence, both ROCK mRNAs were present in the cytoplasm of macrophages, whereas ROCK proteins were undetectable. Macrophage adherence promoted signaling through P-selectin glycoprotein ligand-1 (PSGL-1)/Akt/mTOR that resulted in synthesis of ROCK-1, but not ROCK-2. Following synthesis, ROCK-1 was catalytically active. In addition, there was a rapamycin/sirolimus-sensitive enhanced loading of ribosomes on preformed ROCK-1 mRNAs. Inhibition of mTOR by rapamycin abolished ROCK-1 synthesis in macrophages resulting in an inhibition of chemotaxis and phagocytosis. Macrophages from PSGL-1-deficient mice recapitulated pharmacological inhibitor studies. These results indicate that receptor-mediated regulation at the level of translation is a component of a rapid set of mechanisms required to direct the macrophage phenotype upon adherence and suggest a mechanism for the immunosuppressive and anti-inflammatory effects of rapamycin/sirolimus.

Indexed as

AnimalsCell AdhesionCells, CulturedGene Expression RegulationIntracellular Signaling Peptides and ProteinsMacrophages, PeritonealMaleMembrane GlycoproteinsMiceMice, Inbred C57BLMice, KnockoutModels, BiologicalOncogene Protein v-aktProtein BiosynthesisProtein KinasesProtein Serine-Threonine KinasesIntracellular Signaling Peptides and ProteinsMembrane GlycoproteinsmTOR protein, mouseOncogene Protein v-aktProtein KinasesProtein Serine-Threonine KinasesP-selectin ligand proteinrho-Associated KinasesTOR Serine-Threonine Kinases

Identifiers

PMID17245434
PMCPMC1783463
OpenAlexW2124283941

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.